A Study to Evaluate Safety and Efficacy of BEY1107 in Combination with Temozolomide in Patients with Recurrent or Progressive Glioblastoma Multiforme (GBM)

NCT ID: NCT05769660

Last Updated: 2025-03-10

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: PHASE1
• Total Enrollment: 12 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2022-11-29
• Study Completion Date: 2026-12-31

Brief Summary

This is a Phase 1 study to evaluate the maximum tolerated dose, safety and efficacy of BEY1107 in combination with Temozolomide in Patients with Recurrent or Progressive Glioblastoma Multiforme (GBM)

Detailed Description

In Phase 1, patients with recurrent or progressive glioblastoma multiforme who failed with the standard of care will be enrolled at each dose level of BEY1107 in combination with Temozolomide.

Conditions

Glioblastoma Multiforme

Study Design

• Allocation Method: NA
• Intervention Model: SEQUENTIAL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

BEY1107 + Temozolomide

Administer BEY1107 in combination with Temozolomide, 4-weeks as 1 cycle.

Group Type: EXPERIMENTAL

BEY1107

Intervention Type: DRUG

Administer twice daily, PO, 4-week continuous dose.

Temozolomide

Intervention Type: COMBINATION_PRODUCT

Administer once daily, PO, 5-day continuous dose, followed by 23-day rest period.

Interventions

BEY1107

Administer twice daily, PO, 4-week continuous dose.

Intervention Type: DRUG

Temozolomide

Administer once daily, PO, 5-day continuous dose, followed by 23-day rest period.

Intervention Type: COMBINATION_PRODUCT

Eligibility Criteria

Inclusion Criteria

1. Adult males and females aged over 19 years or older at the time of Informed Consent.

2. Diagnosed with GBM according to the World Health Organization(WHO) criteria.

3. Subjects with progression or recurrence, with no response to the initial standard of care after being confirmed as GBM on histopathology.

4. Subjects with 1 or more lesions that are measurable or evaluable according to the Response Assessment in Neuro-Oncology(RANO) criteria.

5. Subjects with European Cooperative Oncology Group(ECOG) performance status 0 or 1.

6. For Subjects using corticosteroids, those who do not need escalation within at least 2 weeks prior to administration of Investigational Product(IP) and on a stable dose.

7. Women of childbearing potential who are not surgically sterile must consent to practice acceptable contraception until 6 months after the end of IP administration and also have the evidence of not being fertile.

8 Non-vasectomized men who consent to use an acceptable contraception by one-self and the partner until 3 months after the end of IP administration.

9. Subjects who are fully informed of this trial, voluntarily decide to participate in the trial and provide written consent to comply with requirements for the trial.

Exclusion Criteria

1. Patients with a history of chemotherapy for treatment of recurrent glioblastoma multiforme after the initial standard of care as of screening.

2. Subjects who have not recovered from the toxicity of the prior anticancer therapy.

3. Subjects who have past history of major gastrointestinal surgery making oral drug administration impossible or possibly affecting absorption of IP.

4. Subjects who had a major surgery requiring general anesthesia within 4 weeks of screening.

5. Subjects with a history of other malignancy except adequately treated basal cell carcinoma of the skin or cervical carcinoma in situ, papillary thyroid cancer or early gastric cancer.

6. Subjects with a genetic problem(eg. Galactose intolerance).

7. Subjects with hypersensitivity to the ingredient(s) or excipient(s) of the investigational product (BEY1107) or temozolomide.

8. Subjects with hypersensitivity to dacarbazine (DTIC).

9. Subjects who have the cardiovascular disease as of screening.

10. Active hepatitis B, C or HIV positive.

11. Patients with acute or severe infection.

12. Subjects who take a Rifampin, Phenytoin and azole class antifungal drugs in combination.

13. Subjects who had been administered other IP within 4 weeks prior to screening.

14. Patients with inadequate bone marrow, kidney and liver function.

15. Pregnant women, breastfeeding women, or positive findings on the pregnancy test at screening.

16. Subjects with life expectancy of less than 12 weeks by the investigator.

17. Subjects determined by the investigator to be ineligible for participation in this trial.

• Minimum Eligible Age: 19 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

BeyondBio Inc.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Seoul National University Hospital

Seoul, , South Korea

Site Status: RECRUITING

Countries

South Korea

Facility Contacts

Beyondbio Inc.

Role: primary

clinicaltrials@beyondbio.co.kr

+82-42-716-0020

Other Identifiers

BEY-2021-02

Identifier Type: -

Identifier Source: org_study_id